Senior Scientist—Analytical Chemistry & Drug Delivery

MSD; Rahway (NJ); Presencial; USD 117.000 - 184.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical

Dental

Vision care

401(k) Retirement plan

Paid holidays

Vacation

Sick days

Descripción de la vacante

Merck & Co., Inc. in Rahway, NJ, seeks a Senior Scientist to develop analytical methodologies for drug substances and a wide range of dosage forms. You will apply LC/MS, NMR, and other techniques, contributing to regulatory submissions and trial support.

You will collaborate with a global team, lead innovative analyses, and advance drug development in a GMP environment. Travel 5-10% is required.

Formación

• PhD or Master with relevant pharma experience required.
• Strong technical problem solving and publications expected.
• Excellent written and oral communication skills; leadership and collaboration needed.

Responsabilidades

• Develop innovative analytical methodologies for early- to late-phase programs for drug substances and dosage forms.
• Contribute to regulatory submissions and support clinical trials.
• Collaborate across teams to advance drug development using analytical characterization and data analysis.

Conocimientos

Analytical Method Development

Assay Development

Bioanalytical Analysis

Chemistry

Drug Development

GMP Environments

Innovative Thinking

Liquid Chromatography (LC)

Mass Spectrometry (MS)

Method Development

Nuclear Magnetic Resonance (NMR)

Pharmaceutical Industry

Regulatory Submissions

Strategic Thinking

Technical Writing

Educación

PhD in Chemistry, Pharmaceutical Science, or related discipline

Master’s degree in Chemistry, Pharmaceutical Sciences, or related discipline + 3 years pharma experience

Bachelor’s Degree in Chemistry, Pharmaceutical Sciences, or related discipline + 7 years industry experience

Herramientas

LC/GC instrumentation

Mass Spectrometry hardware

Descripción del empleo

Merck & Co., Inc. in Rahway, NJ, seeks a Senior Scientist to develop analytical methodologies for drug substances and a wide range of dosage forms. You will apply LC/MS, NMR, and other techniques, contributing to regulatory submissions and trial support.

You will collaborate with a global team, lead innovative analyses, and advance drug development in a GMP environment. Travel 5-10% is required.